Antimicrobial fabric application system

ABSTRACT

An antimicrobial supply system employs a process water supply and incorporates a metallic ion supply connected to the process water supply to provide a high ion concentrate to an output. A dilution reservoir is connected to the metallic ion supply output and has an input from the process water supply. A pump is connected to an output of the reservoir. A manifold connected to the pump provides a dilute concentrate to at least one washing system. An electronics control module is connected to a first flow controller between the process water supply and the metallic ion supply and a second flow controller between the metallic ion supply and the reservoir for dilution control establishing a desired metallic ion concentration.

REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 16/127,187 filed on Sep. 10, 2018, which is a continuation of Ser. No. 15/629,282 filed on Jun. 21, 2017, which is a continuation of U.S. application Ser. No. 14/460,287 filed on Aug. 14, 2014 and relies on the priority of U.S. Provisional Application Ser. No. 61/912,768 filed on Dec. 6, 2013 having a common assignee with the present application, the disclosure of which is incorporated herein by reference. This application is related to application Ser. No. 14/460,262, filed Aug. 14, 2014, entitled METHOD FOR ANTIMICROBIAL FABRIC APPLICATION, the disclosure of which is incorporated herein by reference.

BACKGROUND OF THE INVENTION Field

The present invention is in the technical field of antimicrobial treatment of fabrics and textile materials. More particularly, the present invention provides a system providing metallic ion generation and dilution, in desired concentrations, for batch storage and entrainment in a flow for use in antimicrobial treatment of fabrics and a method for controlled introduction of the antimicrobial agent into the textile.

Related Art

Shortcomings of existing antimicrobial treatments can lead to stain and odor causing bacteria build-up, mold and mildew as well as the spread of infection through direct contact, airborne disease and waterborne disease. These diseases can be acquired by their victims from contacting contaminated surfaces, breathing air containing pathogens, or drinking pathogen containing water. Contamination of fabrics or textiles in uniforms, surgical scrubs, sheets, blankets, napkins, table cloths and similar materials by microbial pathogens can contribute to spread of disease.

Prior art antimicrobial treatments do not provide effective lasting antimicrobial benefit after the treatment has been administered. Existing antimicrobial treatments can also lead to immunization of evolved pathogens to the respective treatment. Such immunization of evolved pathogens can result in infections which cannot be treated with the conventional treatments that caused the pathogens to become immune.

Enterprises which specifically have problems with microbial issues ranging from bacterial odor through the spread of infectious diseases include, but are not limited to: the cruise line industry, hotel and gaming, professional sports teams, health and fitness clubs, nursing homes, and hospitals. Healthcare facilities currently have a growing problem with immunized pathogens being virtually untreatable with conventional methods. With such hospital infections, the harmful microbes are often carried in the linens and clothing provided by the hospital. Once hospital textiles have been laundered and treated, they are susceptible to recontamination by microbes and pathogens. Pathogens carried by these textiles can infect hospital patients and even cause death. Since almost every patient spends the majority of his or her time in bed, in a gown, between the sheets, this linen environment is the core of the overall hospital environment for the patient, and a primary site in the battle against infection. In the Cruise Ship industry, textiles are ubiquitous on cruise ships, including napkins, tablecloths, aprons, uniforms, towels, and robes.

In the healthcare field antimicrobial fabrics have been employed in which an antimicrobial ingredient is imparted into the threads or fibers during fiber or textile manufacturing. The fibers are embedded, dipped, soaked, or coated with antimicrobial agent during the manufacturing process. However, efficacy declines over time as the antimicrobial agent in the fabric is washed away and never restored.

These methods are not satisfactory for the market. In addition to the efficacy/performance issues listed above and because the textiles are manufactured to already include the beneficial antimicrobial agent such as silver, these products require linen providers to make a large upfront capital investment to purchase new, impregnated linen inventory. Inventory replacement can cost millions of dollars for large industrial laundering businesses. Additionally, the linen's antimicrobial efficacy steadily degrades over time. After each use and wash, the antimicrobial feature is diminished, causing effectiveness to decrease over time. Further, the products are aesthetically unpleasing and uncomfortable to the touch. Linen providers have reported that silver-embedded fabrics can often exhibit an off-white discoloration and are difficult to press.

It is therefore desirable to provide an antimicrobial treatment system which may be employed directly in water supply systems to provide efficacious antimicrobial action in order to transform ordinary textile materials/products into lasting active antimicrobial entities.

SUMMARY OF THE INVENTION

The present embodiment disclosed herein provides an antimicrobial textile treatment system which employs a process water supply. A metallic ion supply provides a high ion concentrate to an output. A dilution reservoir is connected to the metallic ion supply output and has an input from the process water supply. A dosing pump connected to an output of the reservoir. A manifold is connected to the pump providing a dilute concentrate to at least one washing system. An electronics control module is connected to a first flow controller between the process water supply and the dilution reservoir and a second flow controller between the metallic ion supply output and the reservoir.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features and advantages of the present invention will be better understood by reference to the following detailed description of exemplary embodiments when considered in connection with the accompanying drawings wherein:

FIG. 1 is a block diagram representation of the concentrate supply and dilution system;

FIG. 2A is a detailed block diagram of a concentrate supply system;

FIG. 2B is a pictorial view of an embodiment implementing the replaceable concentrate container with a receiver structure in a first installation position;

FIG. 2C is a side section view of the embodiment of FIG. 2B in the first position;

FIG. 2D is a side section view of the embodiment of FIG. 2B with the actuation handle of the receiver structure in motion for piercing of the concentrate container;

FIG. 2E is a side view showing the receiver structure and concentrate container in the in use position;

FIG. 2F is a front section detailed view of the container piercing system in the installation position;

FIG. 2G is a front section detailed view of the container piercing system in the piercing position;

FIG. 2H is a front section detailed view of the container piercing system in the in use position;

FIG. 2I is a front section view of the container piercing system in the in use position;

FIG. 3 is a block diagram of the electronics module control processes;

FIG. 4 is a block diagram of the elements for antimicrobial agent infusion into fabrics;

FIG. 5 is a block diagram of a second embodiment of the concentrate supply and dilution system;

FIG. 6 is a block diagram of a third embodiment of the concentrate supply and dilution system;

FIG. 7 is a block diagram of a high flow capacity system for antimicrobial concentrate supply; and,

FIG. 8 is a block diagram of a direct flow concentrate additional embodiment.

DETAILED DESCRIPTION OF THE INVENTION

The embodiments disclosed herein provide a system for generation and batch dilution of metallic ions for use as an antimicrobial agent in processes such as commercial washing systems to treat textiles. The terms fabric, linen and textile are used interchangeably herein. Referring to the drawings, FIG. 1 shows a concentrate supply and dilution system 10 which is housed in a cabinet 12. The system 10 incorporates an addition column 14 as a dilution reservoir which receives deionized (DI) water through a DI inlet 16 under control of a DI solenoid valve 18. In exemplary embodiments, the addition column 13 may range in size from 0.5-5 L depending on the volumes of the commercial washing system components. An aeration device 20 aerates the incoming DI water flow to provide a desired CO2 concentration in the DI water for enhanced conductance measurements, as will be described subsequently. The addition column 14 receives concentrated antimicrobial agent for dilution from a concentrate supply system 22, described in greater detail subsequently. A solenoid dosing valve 24 controls delivery of antimicrobial agent from the addition column and a dosing pump 26 administers desired amounts of antimicrobial agent from the addition column to a supply outlet 28 for use in a commercial washing system as will be described subsequently. A mixer 30 is employed to maintain an even distribution of DI water and antimicrobial agent in the addition column 14. A conductivity measurement probe 32 provides concentration measurement. A level probe system 34 having an overflow high level sensor 36 a, a dose level sensor 36 b and a reserve level sensor 36 c allows quantity measurement in the addition column 14 for process control. A DI flush line 38 with a flush solenoid valve 40 provides DI water flush of the lines to the washer. A solenoid drain valve 42 is provided to drain the addition column 14. Control of the solenoid valves, mixer and concentrate supply system is accomplished through an electronics control module 44 which receives data input from the conductivity measurement probe 32 and the level probe system 34. An access panel 46 is provided in the cabinet 12 for replacement of concentrate canisters in the concentrate supply system 22.

Details of the concentrate supply system 22 are shown conceptually in FIG. 2A. A concentrate bottle or canister 50 is connectable into a receiver 52 for extraction of concentrated antimicrobial agent contained in the canister. For the embodiments described herein, a metallic silver solution is employed as the antimicrobial agent and may be compounded by employing a selected one of the following processes.

Silver nitrate or silver acetate may be dissolved in deionized water to reach a concentration of up to 1000 g Ag/L solution and stored at room temperature. Silver oxide may be dissolved in dilute nitric acid in the absence of carbon dioxide to a concentration of 25 ppm. For either of these solutions the canister 50 may be a clear container (preferably glass, but polypropylene or similar plastics may be employed).

Silver chloride may to be dissolved in 30% ammonium chloride to a concentration of 3000 g Ag per L solution. Silver Carbonate may be dissolved in dilute nitric acid to a concentration greater than its solubility in pure water of 0.0032 g/100 mL. These solutions are light sensitive (especially UV/sunlight). The canister 50 must therefore be opaque.

Silver sulfate is miscible in sulfuric acid. Silver sulfate can also be dissolved in water up to 0.79 g/100 mL. Silver powder with a particle size of approximately 2 um may be dissolved in dilute nitric acid to a final concentration equivalent to silver nitrate and stored at no lower than room temperature. The canister 50 for either of these solutions may be clear.

The canister 50 incorporates a sealed lid 54 to contain the metallic silver solution as a leak-proof container. A dip tube 56 for extraction of the solution extends from a first quick connect 58, shown integrated in the lid 54 for the embodiment in the drawings. A vent tube 60 extends from a second quick connect 62. The first quick connect and second quick connect provide a connection interface for the canister. The receiver 52 includes a first mating quick connect 64 to engage the dip tube quick connect 58 and a second mating quick connect 66 to engage the vent tube quick connect 62. A vent line 68 extends from the second mating quick connect 66 for venting the canister 50. A feed line 70 extends to the dip tube 56 through connection to the first mating quick connect 64 for delivery of ionic silver solution. A metering pump 72 is connected to the feed line 70 for delivery of the concentrated metallic silver solution to the addition column 14 through conduit 74. In exemplary embodiments, the metering pump is a precision adjustable pump such as an “STH” Low Flow Miniature OEM Pump available from Fluid Metering, Inc., 5 Aerial Way, Suite 500 Syosset, N.Y. 11791. Mixing capability for the canister 50 is employed to maintain a consistent solution of metallic silver concentrate in the canister. For the embodiment shown, a magnetic mixing spinner 76 is contained within the canister 50 and the receiver includes a magnetic driver 78 to activate the mixing spinner. In alternative embodiments, a connected stirring device or a vibratory mixer may be employed. A level indicator 80 is incorporated in the canister 50 to enable an empty warning system which may include bottle change frequency monitoring. Detection methods in the level indicator 80 may include ultrasonic, electro-optic, piezo-resonant, proximity or pressure. An identification element 82 is associated with the canister 50 for identification. A bar code label or similar device with a corresponding scanner may be employed or the identification element may incorporate on-board memory device such as an iButton available from Maxim Integrated, Inc., San Jose, Calif. (see http://www.maximintegrated.com/products/ibutton/ibuttons) that interfaces with the electronics module to carry out desired system functions. The memory device shall be used to track the canister 50 as inventory item, provide process & product trace-ability and shall enable the concentrate supply system 22 to operate, for example provide functional lock-out of operation without an acknowledged canister.

An exemplary embodiment of a receiver structure and associated concentrate container is shown in FIGS. 2B-2I. As seen in FIG. 2B, canister 50 is mounted in receiver 52 in an inverted position with sealed lid 54 as the connection interface engaging a connection element 202. The receiver includes a supporting structure 204 having vertical support arms 206 with lateral spring elements 208 and vertical spring element 210 to support and restrain the canister 50. A rotating cradle 212 supports the connection element 202. A base 214 engages the rotating cradle 212 and incorporates an activation handle 216. Upon activation of the supporting structure for fluid interconnection of the canister 50, as will be described in greater detail subsequently, concentrate from the canister 50 is fed through fitting 218 to the feed line 70 for distribution of the ionic silver solution as described with respect to FIG. 2A.

As seen in FIGS. 2C and 2F, lid 54 incorporates an annular relief 219 which is received in an annular crown 220 on the connection element 202 to support the container and lid in the receiver. An o-ring seal 222 or similar sealing arrangement provides a seal between the relief 218 and the crown 220. A pierceable nipple 224 in the lid 54 is received within the crown 220 for communication with a feed conduit 226 terminating in the fitting 218. A piercing pin 228 is reciprocally mounted in the connection element 202 and is activated by a cam 230 interconnected to the activation handle 216. As shown in FIG. 2C with the handle in the “down” position for insertion of the container 50, the container is inserted in the receiver with the lid 54 engaged by the crown 220 on the connection element 220. The piercing pin 228 is retracted at the bottom of travel and the rotating cradle 212 is in a lowered position.

Upon an initial portion of rotation of the activating handle 216 as shown in FIGS. 2D and 2G, cam 230 is rotated to cause the cam lobe to reciprocate piercing pin 228 upward to contact and pierce the nipple 224 in the lid 54 of container 50. Upon continued rotation of the activating handle 216 to an “up” position as shown in FIGS. 2E and 2H, cam 230 has further rotated the lobe past piercing pin 228 allowing the pin to retract thereby placing the pierced container nipple 219 in fluid communication through conduit 226 to fitting 218. A second cam 232, best seen in FIG. 2I, is rotated by the handle 216 for contact to urge connection element 202 upward supported by rotating cradle 212. For the embodiment shown, a spring 234 interengages the second cam 232 and connection element 202. As shown in FIG. 2I, upon elevation of the container 50 by the connection element 202 and rotating cradle 212, a vent pin 236 restrained by a support column 238 is engaged to pierce the container wall 240 thereby venting the container for flow of concentrate.

Referring to both FIGS. 1 and 2A, standard operation of the concentrate supply and dilution system 10 for delivery of antimicrobial agent to a wash system is accomplished by opening column DI fill solenoid 18 and fill the addition column 14 until high level probe 36 a is triggered. Metered addition of concentrate from the canister 46 is accomplished using precision metering pump 72 into the column 14. The conductance level probe 32 is de-energized and mixing is accomplished using mixer 30. The conductance level probe 32 is then activated for measurement to confirm the desired concentration of antimicrobial agent has been achieved. Dosing of diluted concentrate from the addition column 14 to the washer is then accomplished by opening the dosing solenoid valve 24 and turning on the dosing pump at a predetermined speed so that the dose is administered a predetermined dosing period, as indicated by the dose-level probe 36 b dis-engagement from the solution. In exemplary embodiments the dosing period is 20-30 seconds. It may be desirable to vary the dosing rate during a dosing period. The dosing period is established to ensure uniformity of silver uptake in the textiles. The solenoid dosing valve is then closed and the dosing pump turned off. Flushing of the dosing pump and line to washer is then accomplished by opening the DI dosing line flush valve 40 and turning on the dosing pump. Upon completion of the line flush, the DI dosing line flush valve 40 is closed and the dosing pump 26 is turned OFF.

The functional operational aspects of the electronics control module 44 are shown in detail in FIG. 3. A system controller 84, which may be a microprocessor or similar device incorporated with the electronics control module 44 mounted in the cabinet 12, and a display 86 for interaction with an operator provide control for the concentrate supply and dilution system. In exemplary embodiments a Arduino Mega single board computer is employed. Alternatively, a laptop computer or similar device may be employed which incorporates one or both of the system controller and display requirements. A panel with control buttons 88 is employed on the cabinet 12 for input by the operator for control of various aspects of the system operation such as initial high concentration dosing, calibration, normal concentration dosing or system bypass for manual dosing. Another input could be the mass of the textiles which the software uses to calculate the final mg/kg of Ag+ needed. In various embodiments the control buttons may be incorporated on the display as a touch screen or for alternative employing a laptop or other computer, the keyboard may provide the control button functions. A remote panel 90 at an alternative location interfacing with the system controller 84 under wired or wireless connection may also be supplied for remote control input. A power supply 92 provides power conversion from standard AC line input to DC voltages for solenoid operation and microprocessor and display power. A receiver control 94 incorporates hardware for processing of input from the identification element 82, the low level sensor 80 and for operation of the magnetic driver 78 and associated mixing spinner 76. A micro-pump controller 96 receives instructions from associated software routines in the system controller 84 for operation of the metering pump 72 and a silver concentrate controller 98 connected to the conductivity measurement probe 32, which interprets conductivity measurements and translates them into silver concentration readings so that the system controller 84 may interactively control addition of silver concentrate from the canister 50 to the addition column 14. An addition column functional I/O grouping 100 incorporates hardware and software routines in the system controller for operation of the functions of the addition column 14 including operation of the mixer 30, detection of overflow, dose and reserve fill quantities through connection to level probes 36 a and 36 b and 36 c. The exemplary system described herein has no hardware component for empty level control; rather it is determined in software (timing based functions) in reference to extended periods of inactivity by the reserve level sensor. At the point of inactivity, the system drains, resets and fills the column 14 with DI and looks for the reserve level sensor 36 c to trigger. If no fill is detected, an alarm signals. The column is not drained until empty during normal operation in order to maintain wetting of the concentration probe 32. Dry to fill could result in air bubble formation on the surface of the concentration probe 32, leading to false readings. Fill of the addition column by control of solenoid valve 18 is accomplished by the addition column controller. Flushing of the additional column to the commercial washer system is accomplished by a dosage line functional grouping 102 which controls operation of solenoid valve 24 and the dosing pump 26 upon instruction from the system controller 84. A commercial washer system interface 104 receives data from the commercial washer system, as will be described subsequently, for status to allow proper timing and operation of the flushing of the addition column, lines flush and DI water fill input. A second silver concentrate controller 105 receives input from a silver concentrate sensor in the commercial washer system for communication to the system controller 84 which may then adjust delivery of concentrate and relative dilution of the concentration to obtain a desired ultimate concentration in the commercial wash system. A memory 106 is employed by the controller for software routines storage and random access memory for process and sequence data.

Infusion of the antimicrobial silver concentrate into textiles is accomplished using system elements as shown in FIG. 4. Silver ions are naturally antimicrobial. When treated with silver, textiles exhibit antimicrobial efficacy and fight off bacteria fungi and virus. In order to produce antimicrobial characteristics, the textile must be treated with and maintain a certain minimum silver content, across the entire textile, which can be specified and measured in terms of mg Ag per kg textile. The silver content can be measured with inductively coupled plasma (ICP) down to 0.25 mg Ag per kg textile. Silver-treated textiles must maintain at least 0.75 mg Ag per kg textile to achieve antimicrobial efficacy. As the content of silver increases relative to textile weight, the antimicrobial efficacy increases. For example, 0.75 mg Ag/kg may kill 99.9% S. aureus 24 hours, while 3 mg Ag/kg may kill 99.9% S. aureus in 30 minutes. As the surface area of different textiles vary, an additional amount of Ag may be needed. However, to avoid discoloration of the textiles, metallic ion concentration at a maximum of 100 mg Ag per 1 kg textiles is introduced by the system into the basin

During the treatment process, silver attaches to textile via electrostatic dipole interactions. The positive charge from the silver ions is attracted to the slight-negative dipole on the polymer backbone of textile fibers. For example, cotton sheets are composed of cellulose monomers which contain a number of oxygen molecules which are electronegative. The electronegativity of the oxygen molecules are a target active site for the positively charged silver ion. A similar interaction is observed between silver ions and the “ester” group on polyester textile. The ester is composed of a carbonyl oxygen (carbon double bonded and singly bonded to oxygen). Through use of deionized water in the present system, removal of contaminants creates a greater probability that silver ions will affix to reactive bonding sites on the textile's polymer chains as opposed to cationic contaminants and similarly, reduction of the probability of anionic contaminant's reactions to silver ions. Also the higher concentration of silver ions in solution creates driving force for the ions to bond with electronegative dipoles.

Affinity of silver to textile's electronegatively charged dipoles is high. Thus, highly concentrated solution will result in unevenly coated silver ions on the fabric, as a result of ‘first come, first serve’ behavior of reactive dipole-to-textile attraction. To overcome this, a standing bath of pure DI water is created and clean textiles are submerged in the bath. Agitation is then initiated and ionic silver solution is administered over the duration of at least 20 seconds of agitation of the bath to evenly coat submerged textile; additional agitation of up to 2 minutes following silver administration will help smooth out uniformity of silver across the treated textiles. Submersion forces a minimum volume:mass ratio between DI+Ag solution and textile material, regardless of treatment basin geometry. In an exemplary embodiment, the basin moves relative to the textile load, causing the textile shape to modulate, forcing the fluids to completely exchange throughout the volume such as in a rotating drum.

As seen in FIG. 4, a wash basin 110, which may be a standard rotating wash tub of a commercial washing system, receives textiles 112. As defined herein the wash basin may be a single basin for use in detergent addition cycles and rinse cycles or may be separate dedicated detergent or rinse cycle basins and the dosing of antimicrobial agent may be in either a detergent addition cycle or a rinse cycle to implement the treatment. By operation of the solenoid valve 40 in the concentrate supply and dilution system 10 to supply DI water through DI flush 38 and pump 26 to the outlet 28 wash basin 110 is filled with DI water to establish the standing bath for contained textiles 112. Agitation of the wash basin 110 is then initiated and the desired ionic silver solution concentration is delivered from the concentrate supply and dilution system by operation of solenoid dosing valve 24 and dosing pump 26. The dosing pump 26 is variable speed or is of fixed speed and is sized to provide full dosing of the ionic silver solution concentration from the addition column 14 over the desired dosing period for even coating of the submerged textiles 112. A second silver concentration sensor 113 may be inserted in the commercial wash basin or tunnel for measurement of actual dosed concentration. Output of the sensor 113 is provided to the second silver concentrate controller 105 for communication to the electronics control module as previously described (individual connections between control and monitoring components and the electronics control module are not shown to allow clarity in the drawing). Different textile compositions may require modified dosing periods or concentrations to maximize the efficacy of the antimicrobial action. The system controller in the electronics control module may be programmed to accommodate varying textile compositions through identified input from the user interface (UI) for a particular textile type with predetermined dosing period and concentration settings. Alternatively, manual input through the UI may be employed for concentration and/or dosing period to accommodate required alternative textile settings as described subsequently.

Retention characteristics of silver ions in textiles during multiple wash cycles has demonstrated that an initial treatment with higher silver ion concentration, approximately a factor of 4 over standard treatment concentrations provides a higher starting point to maintain silver ion retention in the textiles for increased efficacy of the antimicrobial action in the textiles. The ultimate asymptotic level of silver ion content in textile is roughly a factor of 4 over the standard treatment on mass silver per mass textile basis.

For additional control of diluted concentration of the antimicrobial silver ion concentrate in the addition column 14 supplemental elements may be added as shown in FIGS. 5 and 6. In FIG. 5, a drain standpipe 114 having an entrance level consistent with the high level sensor 36 a and an exit to a drain 116 is provided in the addition column 14. During addition of DI water to the addition column using solenoid valve 18 high level sensor 36 a provides control input to the electronics control module 44 to close solenoid valve 18 upon DI water fill to that level (individual connections between control and monitoring components and the electronics control module are not shown to allow clarity in the drawing). However, any excess fill due to delay or hysteresis in closing of the valve is avoided since any overflow will be directed through the drain standpipe. An exact quantity of DI water is then present in the addition column 14 for concentrate metering by metering pump 72 from the canister 50 into the addition column. Mixing and concentration measurement may then be accomplished as previously described for the embodiment of FIG. 1.

Similarly in FIG. 6, addition column 14 incorporates a precision volume insert 118 into which DI water is introduced through supply solenoid valve 18. The DI water in the precision volume insert 118 is allowed to overflow into the addition column 14 until an overflow level indicated by high level sensor 36 a is reached. The level indication from the high level sensor 36 a to the electronics control module 44 results in closing of solenoid valve 18 (individual connections between control and monitoring components and the electronics control module are not shown to allow clarity in the drawing). An exact quantity of DI water is then present in the precision volume insert 118 for concentrate metering by metering pump 72 from the canister 50 directly into the precision volume insert in the addition column. Mixing and concentration measurement may then be accomplished as previously described for the embodiment of FIG. 1. Upon depletion of the precision metering column through solenoid valve 24 and dosing pump 26, overflow present in the addition column may be released through solenoid valve 120 through dosing pump 26 to flush the inlet line 28 into the washer system to obtain a complete accurate dose of the diluted concentrate from the addition column without any additional diluted antimicrobial agent.

A high flow rate washer basin fill system employing the concentrate supply and dilution system is shown in FIG. 7. A treatment system 119 employs agranulated activated carbon (GAC) filter 120 receiving water from the house soft water source 122. Water drawn from the GAC flows through a reverse osmosis (RO) filter 124 and into a deionizing (DI) mixed-bed resin 126 from which process DI water is provided to a storage tank 128, for exemplary embodiments a 400 gal tank, from which DI water is supplied through high volume pump 130. Treating water from the house soft water source is accomplished to control total dissolved solids (TDS) to a level <300TDS. A return flow through solenoid valve 132 allows flow rate and pressure to be maintained without pump startup delay. DI water may then be supplied from the pump 130 directly to the tunnel washer 134 or to the concentrate supply and dilution system 12 through solenoid valve 18 for introduction of antimicrobial agent as previously described.

As an alternative to use of a dilution reservoir or addition column, antimicrobial silver concentrate may be mixed directly into a water supply stream as shown in FIG. 8. As for the embodiment described with respect to FIG. 7, treatment of a house water supply is provided by a treatment system employing a granulated activated carbon (GAC) filter 120 receiving water from the house soft water source 122. Water drawn from the GAC flows through a reverse osmosis (RO) filter 124 and into a deionizing (DI) mixed-bed resin 126 from which process DI water is provided through a control valve 140 and a flow meter 142 connected to the electronics control module 44 for control and monitoring (individual connections between control and monitoring components and the electronics control module are not shown to allow clarity in the drawing). As previously described for the prior systems, concentrate from canister 50 is provided through metering pump 72. A second flow meter 144 for confirmation of the flow through the metering pump may be employed. Flow from the control valve 140 and metering pump 72 are combined in a venturi mixer 146 for direct mixing of the concentrate into the incoming water flow. A conductivity probe 148 provides actual resulting concentration to the electronics control module 44 for control of the metering pump 72 and control valve 140 to obtain desired concentration in the mixed water solution provided from the venturi mixer to the wash basin 110. Control by the electronics control module of the metering pump 72 is employed to provide the desired dosing time as a portion of a fill cycle for the wash basin through the control valve 140 with associated control of agitation of the wash basin as previously described. Alternately, the output of the venture mixer may be used with a holding column and then dosed as previously described.

Standard operation of the concentrate supply and dilution system has been previously described. The system control capability provided by the electronics control module 44 allows great flexibility in operation of the system to provide various process features. Normal operations include, column flush, column calibration, metering pump calibration, measurement probe calibration, canister new/replacement, metering pump purge, flush dosing line, initial concentration addition full cycle operation, standard concentration addition full cycle operation and manual addition for standard, initial and custom processes. The electronics control module with the associated controller and display may provide alarms, data recording and other operational screen displays.

A column flush is accomplished by opening DI fill solenoid valve 18 to fill the addition column 14 to high level sensor 36 a. Drain valve 42 is then opened to drain the addition column 14 and then closed. This fill and drain process is repeated two times. The DI fill solenoid valve 18 is then controlled to fill to the addition column 14 to the high level sensor 36 a. The operator then provides a manual input to acknowledge that the dosing line 28 is configured for flush. Dosing valve 24 is then opened and dosing pump 26 is turned on for a predetermined time for complete flush of the line 28 and/or washing system. Dosing pump 26 is then turned off and dosing valve 24 is closed. The DI flush valve 40 is then opened and dosing pump 26 is activated for a predetermined time for DI flush. The dosing pump 26 is then turned off and DI flush valve 40 is closed. The display then shows a task complete message.

Column calibration is accomplished for the addition column by metering a predetermined quantity of antimicrobial concentrate from the canister 50 into the addition column 14 to ensure conductivity measurement by the level sensing probes 36 a, 36 b, 36 c. Verification of reservoir volume may be accomplished starting with solution absent from the column. Verification of the reservoir volume is accomplished with each test cycle and step in the cycle prompted from the user interface (UI) provided by the display 86 and control panel buttons 88 as previously described. DI fill solenoid 18 is opened until water level contact with the dose level probe 36 b occurs. Drain valve 42 is opened until the reservoir level probe 36 c is disengaged. Dosing line 28 is temporarily routed into a volume measurement device such as a graduated cylinder. Dosing valve 24 is opened and dosing pump 26 turned on for 1 minute to ensure all solution is pumped out of the column as verified by the operator. This process is repeated adjusting pump timing and reservoir level probe location until target volume is achieved. Dosing valve 24 is then closed and dosing pump 26 turned off. Complete reservoir volume is measured by the fluid in the graduated cylinder.

Verification of delivery volume may be accomplished at the conclusion of the reservoir volume test cycle. Verification of the delivery volume is then accomplished with each test cycle and step in the cycle prompted from the user interface (UI) provided by the display 86 and control panel buttons 88 as previously described. DI fill solenoid 18 is opened until water level contact with the dose level probe 36 a occurs. Dosing line 28 is temporarily routed into a volume measurement device such as a graduated cylinder. Dosing solenoid valve 24 is opened and dosing pump 26 turned on. Dosing valve 24 is closed and pump 26 turned off when low level probe 36 b is reached. This process is repeated adjusting pump timing and low level probe location until target volume is achieved. The process is then repeat two times for confirmation when target volume is achieved

Metering pump calibration is accomplished by temporarily routing outlet conduit 74 into an analytical balance. Manual setting is enabled and/or engagement of standard pump rate at the UI with fixed RPM on the metering pump 72 for Initial and Standard addition. Selectable run times are enabled in increments of 10 sec. “Initial” or “Standard” is selected for pump run mode. The metering pump is then activated for the pre-set time and delivery quantity confirmed on the analytical balance. A prompt for repeat may be provided or the UI may return to home screen.

Conductivity measurement probe calibration is accomplished by occasional auto-calibration and occasional manual calibration.

Canister new/replacement is accomplished as prompted by the UI. In an exemplary embodiment, a yellow alarm is activated when the canister 50 reaches a low level designation by the level sensing device 80, (for example indicating one day of operation remaining) A red alarm is activated and a system stop (system deactivation) when the canister reaches 200 addition cycles after the low level alarm. Installation of a canister 50 into the receiver 52 is accomplished by switching the system to OFF or HOLD. The old canister removed and the new canister is connected to the receiver plumbing and electronics. The system acknowledges the new canister, (manual button or auto barcode/sensor or on-board memory device 82 read as previously described) and is then ready to operate. Separately, a small additional volume in 202 is sized sufficiently to allow continuous use while changing the bottle. For example, if 1 mL were used per cycle, the extra volume would be 30 mL to allow 30 additional minutes to operate.

Metering pump purge is accomplished when necessary by opening column drain valve 42 and turning on the metering pump for 30 seconds. The metering pump is then turned off. An addition column flush is instituted with drain valve 42 closed by opening DI fill valve 18 until the overflow probe 36 a is activated then opening drain valve 42. The addition column flush is then repeated two times.

Flush dosing line is accomplished by opening the DI dosing line flush valve 40 and turning on the dosing pump 26 for a predetermined time based on line volume. The DI dosing line flush valve 40 is then closed and the dosing pump turned off.

Conductivity level probes 36 a, 36 b and 36 c may not “see” DI water on first fill of the addition column that has no residual Ag+ due to lack of conductance. A supplemental float indicator for high level indication may be employed and a first fill to trigger the float indicator with a metering pump addition that will obtain Ag+ concentration the same as an initial dose accomplished. The addition column may then be drained to the low level probe 36 b before beginning normal cycles.

Operational application requires that the system is capable of creating SC solution deliveries in either Standard or Initial dose concentrations from a variety of pre-existing solution concentration states. The system is capable of producing Initial or Standard concentration SC solutions from concentrations of 0 concentration, Standard concentration or Initial concentration states as shown in Table 1 below.

TABLE 1 Addition type Dosing Scenario Target Delivery Volume 4 Startup - Std 643 5 Startup - Initial 1930 0 Std to Std 429 1 Std to Initial 1715 2 Initial to Std 0 3 Initial to Initial 1286

In the following example, the Initial SC solution is created from a 0 concentration state. Upon receipt of a cycle signal from the washer system interface 104 in the electronics control module initial textile dose addition is accomplished by opening the addition column DI fill solenoid valve 18 is opened for approximately 10 sec until the reservoir level probe 36 c is triggered. Metered addition of concentrate from the canister 50 is accomplished with precision pump 72 into the addition column (<60 sec) providing an addition of 1930 uL of concentrate. Simultaneously, DI fill solenoid valve 18 is opened for approximately 10 sec until the dose level probe 36 a is triggered. The conductance measurement probe 32 is de-energized and the mixer 30 energized for 30 seconds. After 20 sec of mixing, the conductance measurement probe 32 is energized and conductance of the diluted concentration is measured during final 10 sec. Upon confirmation of proper concentration, the addition column product is dosed to the washer by opening dosing solenoid valve 24 and turning on dosing pump 26 until reservoir level probe 36 b is dis-engaged from solution. As previously described, the dosing pump is sized to provide the dose within a predetermined dosing period for optimum silver uptake in the textiles. The dosing valve 24 is then closed and dosing pump 26 turned off. The dosing pump and line are then flushed to extract all of the Ag intended to be used in the washer by opening DI dosing line flush valve 40 (based on line volume) and turning dosing pump 26 on (based on line volume). The DI dosing line flush valve 40 is then closed and the dosing pump 26 turned off.

For standard silver ion concentration addition from a standard reservoir concentration state, DI fill solenoid valve 18 is opened (<10 sec) to fill the addition column until dose level probe is triggered. Simultaneously, metered addition of concentrate from canister 50 is accomplished with precision pump 72 into the addition column (<10 sec) providing an addition of 429 uL of concentrate. The conductance measurement probe 32 is de-energized and the mixer 30 energized for 30 seconds. After 20 sec of mixing, the conductance level probe 32 is energized and conductance of the diluted concentration is measured during final 10 sec. Upon confirmation of proper concentration, the addition column product is dosed to the washer upon receipt of a cycle signal from the washer system interface 104 in the electronics control module by opening dosing solenoid valve 24 and turning on dosing pump 26 until reservoir level probe 36 b is dis-engaged from solution. As previously described, the dosing pump is sized to provide the dose within a predetermined dosing period for optimum silver uptake in the textiles. The dosing valve 24 is then closed and dosing pump 26 turned off. The dosing pump and line are then flushed to washer by opening DI dosing line flush valve 40 (based on line volume) and turning dosing pump 26 on (based on line volume). The DI dosing line flush valve 40 is then closed and the dosing pump 26 turned off.

For the concentrate supply and dilution system as described with respect to FIG. 1 the ullage remaining in the addition column, i.e. the volume of fluid present between the reservoir level probe 36 b volume and the empty column, requires modification of the concentrate addition to achieve desired diluted concentrate properties when shifting between an initial treatment and standard treatment concentrations (as an example 3× dosage for initial and 1× dosage for standard) as previously shown in Table 1. The controller 84 in the electronics control module provides process data sequence storage in memory 106 to allow variation of the added concentrations from the canister to the addition column. For example, if an exemplary system employs an addition column of 1.5 L with an ullage of 0.5 L and a normalized standard concentration level for textile treatment of 1.0, if the system has been running standard concentration fills, the reserve fluid in the ullage will have a volume of 0.5 L with a silver concentration of 1.0 at the conclusion of a 1.01 dose delivered to the wash system. Adding the DI water to the addition column for a full 1.5 L requires the addition of a 1.0 dose of silver yielding a 1.0 concentration level for the entire 1.5 L column. Delivery of a 1.0 dose then leaves the ullage with 0.5 L again at a concentration of 1.0. If an initial concentration dose for treatment of textiles is then desired, starting with an ullage of 0.5 L with a concentration of 1.0 adding the 1.0 L of DI water to the addition column then requires addition of a 4.0 dose of silver to yield the desired 3.0 concentration in the 1.5 L total volume for an initial textile treatment. Upon delivery of the 1.0 liter dose, the ullage now contains 0.5 L with a 3.0 concentration. If an additional initial textile treatment dosage is then desired, the 1.0 L fill of DI into the addition column only requires a 3.0 dose of silver to yield a 3.0 concentration in the 1.5 L volume. However, if a standard treatment is desired after an initial treatment dose, the 0.5 L ullage with a 3.0 concentration upon filing to the 1.5 L volume requires a 0.0 dose of silver achieve the desired 1.0 concentration. Upon delivery of a 1.0 L dose to the washer, the ullage again has a 1.0 concentration remaining.

Manual addition of desired diluted concentrate to the commercial washer system may be accomplished through the UI for either the standard or initial concentration levels. In exemplary systems, the UI may additionally provide the ability to alter metering pump activation times for custom concentration dosing. The system can create any concentration of dose desired by controlled Interaction between concentrate canister and addition column by the electronics module, within the limits of the metering pump resolution. A dose volume is set by the difference in volume defined by volume in the addition column defined by level sensors 36 b and 36 c. Responsive to a desired concentration input through the UI, the system controller in the electronics module calculates the amount of concentrate required to produce the desired diluted concentration in the addition column. Operation of the metering pump is controlled by the electronics module to supply that amount of concentrate. Feedback to the system controller from the level sensors and concentration probe during DI fill and concentrate metering is accomplished to determine if a predetermined dose acceptance criteria is met. If the desired concentration is not met, the system controller may issue an alarm, system dump or system correction. For example, if a low concentration is detected, operation to meter more concentrate into the addition column may be undertaken and re-measurement by the concentration probe. If concentration is too high either add more DI or dump to reserve level and start dose over.

Having now described the invention in detail as required by the patent statutes, those skilled in the art will recognize modifications and substitutions to the specific embodiments disclosed herein. Such modifications are within the scope and intent of the present invention as defined in the following claims. 

We claim:
 1. An antimicrobial treatment system comprising: a user interface for receiving input from an operator via the antimicrobial treatment system; an antimicrobial agent supply providing an antimicrobial agent to a supply output; a reservoir connected to the antimicrobial agent supply output and comprising a reservoir output; a pump connected to the reservoir output; a sensor, wherein the sensor detects an operational parameter of the antimicrobial treatment system; and an electronics control module connected to the user interface and the sensor, wherein the electronics control module modifies a control parameter of one or more components of the antimicrobial treatment system in response to at least one of: (i) the received operator input; and (ii) the detected operational parameter of the antimicrobial treatment system.
 2. The antimicrobial treatment system of claim 1, wherein the user interface comprises a remote interface.
 3. The antimicrobial treatment system of claim 1, wherein the antimicrobial agent supply comprises a leak proof container, and the antimicrobial agent comprises a high ion metallic concentrate.
 4. The antimicrobial treatment system of claim 1, wherein the detected operational parameter comprises an operational error in the antimicrobial treatment system.
 5. The antimicrobial treatment system of claim 1, wherein the modified control parameter comprises an alarm signaled by the antimicrobial treatment system.
 6. The antimicrobial treatment system of claim 5, wherein the signaled alarm is displayed via the user interface of the antimicrobial treatment system.
 7. The antimicrobial treatment system of claim 6, wherein the user interface comprises a remote interface.
 8. The antimicrobial treatment system of claim 1, wherein the modified control parameter comprises an operational correction by the antimicrobial treatment system.
 9. The antimicrobial treatment system of claim 1, wherein the modified control parameter comprises a system deactivation by the antimicrobial treatment system.
 10. The antimicrobial treatment system of claim 1, wherein the modified control parameter comprises emptying one or more of the components of the antimicrobial treatment system.
 11. The antimicrobial treatment system of claim 1, wherein the modified control parameter comprises flushing one or more of the components of the antimicrobial treatment system.
 12. The antimicrobial treatment system of claim 1, wherein the sensor is connected to the reservoir.
 13. The antimicrobial treatment system of claim 1, wherein the sensor comprises a concentration sensor.
 14. The antimicrobial treatment system of claim 13, wherein the electronics control module incorporates a controller receiving input from the concentration sensor, and the controller is adapted to operate the one or more components of the antimicrobial treatment system for an operating period calculated to provide a desired concentration of the antimicrobial agent in the reservoir.
 15. The antimicrobial treatment system of claim 1, wherein the sensor comprises a reservoir level sensor.
 16. The antimicrobial treatment system of claim 15, wherein the electronics control module incorporates a controller receiving input from the reservoir level sensor, and the controller is adapted to operate the one or more components of the antimicrobial treatment system for an operating period calculated to provide a desired amount of the antimicrobial agent in the reservoir.
 17. The antimicrobial treatment system of claim 1, wherein the sensor comprises a low level sensor.
 18. The antimicrobial treatment system of claim 17, wherein the electronics control module incorporates a controller receiving input from the low level sensor, and the controller is adapted to operate the one or more components of the antimicrobial treatment system for an operating period calculated to provide a desired amount of the antimicrobial agent in the reservoir.
 19. The antimicrobial treatment system of claim 1, wherein the sensor comprises a dose level sensor.
 20. The antimicrobial treatment system of claim 19, wherein the electronics control module incorporates a controller receiving input from the dose level sensor, and the controller is adapted to operate the one or more components of the antimicrobial treatment system for an operating period calculated to provide a desired dose of the antimicrobial agent in the reservoir. 